Three-Dimensional (3D) Ordered Macroporous Bimetallic (Mn,Fe) Selenide/Carbon Composite with Heterojunction Interface for High-Performance Sodium Ion Batteries

材料科学 复合数 阳极 异质结 双金属片 硒化物 化学工程 碳纤维 纳米技术 电极 金属 复合材料 光电子学 物理化学 冶金 化学 工程类
作者
Jiuwu Wang,Xianfeng Yang,Caini Yang,Danhui Yi,Siyao Chen,Xuping Sun,Chenguang Huang,Yinping Wu,Yue Situ,Hong Huang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (33): 40100-40114 被引量:10
标识
DOI:10.1021/acsami.3c07951
摘要

Transition-metal selenides have captured significant research attention as anode materials for sodium ion batteries (SIBs) due to their high theoretical specific capacities and excellent electronic conductivity. However, volumetric expansion and inferior cycle life still hinder their practical application. Herein, a three-dimensional (3D) ordered macroporous bimetallic (Mn,Fe) selenide modified by a carbon layer (denoted as 3DOM-MnFeSex@C) composite containing a heterojunction interface is fabricated through selenizing a 3D ordered macroporous Mn-based Prussian Blue analogue single crystal. The 3DOM-MnFeSex@C exhibits hierarchically porous architecture with enhanced mass-transfer efficiency; MnSe and FeSe2 particles are encapsulated into macroporous carbon framework, which can significantly promote the electronic conductivity and maintain the structural integrity. The density functional theory calculation indicates that the heterojunction interface between MnSe and FeSe2 has been successfully engineered so that Na+ can be readily adsorbed and rapidly converted, thus promoting the reaction kinetics and extending the cyclic life. As expected, the 3DOM-MnFeSex@C composite delivers excellent rate performance (277.6 mA h g–1 at 10 A g–1), and prolonged cycling life (191.6 mA h g–1 even after 1000 cycles at 2 A g–1) as a sodium storage anode. The sodium storage mechanism of the composite was further investigated by in situ X-ray diffraction and ex situ high-resolution transmission electron microscopy characterization techniques.
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